Vivid PMMA Amann Girrbach System 12(H) A2 (UDI Q250270)
Manufactured by PEARSON DENTAL SUPPLIES, INC.
Device Regulatory Overview
The Vivid PMMA Amann Girrbach System 12(H) A2 (Model/Catalog Number: Q250270) is a medical device manufactured by PEARSON DENTAL SUPPLIES, INC.. This product is indexed under FDA Product Code / Category Classification ELL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Q250270
- Product Code / EMDN
- ELL
- Device Name
- 18(H) A2
- Database Sync Date
- 2026-08-09 09:15:03
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Vivid PMMA Amann Girrbach System 12(H) A2?
The registered manufacturer of record for Vivid PMMA Amann Girrbach System 12(H) A2 is PEARSON DENTAL SUPPLIES, INC..
What is the Primary UDI-DI identifier for Vivid PMMA Amann Girrbach System 12(H) A2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Q250270.
What classification code is assigned to this device?
This device is registered under product classification code ELL.
Similar Classification Devices (ELL)
Other Devices by PEARSON DENTAL SUPPLIES, INC.
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